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Development of smart anti-glycan reagents using immunized lampreys
Studies on the expression of cellular glycans are limited by a lack of sensitive tools that can discriminate specific structural features. Here we describe the development of a robust platform using immunized lampreys (Petromyzon marinus), which secrete variable lymphocyte receptors called VLRBs as...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7048801/ https://www.ncbi.nlm.nih.gov/pubmed/32111965 http://dx.doi.org/10.1038/s42003-020-0819-2 |
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author | McKitrick, Tanya R. Goth, Christoffer K. Rosenberg, Charles S. Nakahara, Hirotomo Heimburg-Molinaro, Jamie McQuillan, Alyssa M. Falco, Rosalia Rivers, Nicholas J. Herrin, Brantley R. Cooper, Max D. Cummings, Richard D. |
author_facet | McKitrick, Tanya R. Goth, Christoffer K. Rosenberg, Charles S. Nakahara, Hirotomo Heimburg-Molinaro, Jamie McQuillan, Alyssa M. Falco, Rosalia Rivers, Nicholas J. Herrin, Brantley R. Cooper, Max D. Cummings, Richard D. |
author_sort | McKitrick, Tanya R. |
collection | PubMed |
description | Studies on the expression of cellular glycans are limited by a lack of sensitive tools that can discriminate specific structural features. Here we describe the development of a robust platform using immunized lampreys (Petromyzon marinus), which secrete variable lymphocyte receptors called VLRBs as antibodies, for generating libraries of anti-glycan reagents. We identified a wide variety of glycan-specific VLRBs detectable in lamprey plasma after immunization with whole fixed cells, tissue homogenates, and human milk. The cDNAs from lamprey lymphocytes were cloned into yeast surface display (YSD) libraries for enrichment by multiple methods. We generated VLRB-Ig chimeras, termed smart anti-glycan reagents (SAGRs), whose specificities were defined by microarray analysis and immunohistochemistry. 15 VLRB antibodies were discovered that discriminated between linkages, functional groups and unique presentations of the terminal glycan motif. The development of SAGRs will enhance future studies on glycan expression by providing sequenced, defined antibodies for a variety of research applications. |
format | Online Article Text |
id | pubmed-7048801 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-70488012020-03-05 Development of smart anti-glycan reagents using immunized lampreys McKitrick, Tanya R. Goth, Christoffer K. Rosenberg, Charles S. Nakahara, Hirotomo Heimburg-Molinaro, Jamie McQuillan, Alyssa M. Falco, Rosalia Rivers, Nicholas J. Herrin, Brantley R. Cooper, Max D. Cummings, Richard D. Commun Biol Article Studies on the expression of cellular glycans are limited by a lack of sensitive tools that can discriminate specific structural features. Here we describe the development of a robust platform using immunized lampreys (Petromyzon marinus), which secrete variable lymphocyte receptors called VLRBs as antibodies, for generating libraries of anti-glycan reagents. We identified a wide variety of glycan-specific VLRBs detectable in lamprey plasma after immunization with whole fixed cells, tissue homogenates, and human milk. The cDNAs from lamprey lymphocytes were cloned into yeast surface display (YSD) libraries for enrichment by multiple methods. We generated VLRB-Ig chimeras, termed smart anti-glycan reagents (SAGRs), whose specificities were defined by microarray analysis and immunohistochemistry. 15 VLRB antibodies were discovered that discriminated between linkages, functional groups and unique presentations of the terminal glycan motif. The development of SAGRs will enhance future studies on glycan expression by providing sequenced, defined antibodies for a variety of research applications. Nature Publishing Group UK 2020-02-28 /pmc/articles/PMC7048801/ /pubmed/32111965 http://dx.doi.org/10.1038/s42003-020-0819-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article McKitrick, Tanya R. Goth, Christoffer K. Rosenberg, Charles S. Nakahara, Hirotomo Heimburg-Molinaro, Jamie McQuillan, Alyssa M. Falco, Rosalia Rivers, Nicholas J. Herrin, Brantley R. Cooper, Max D. Cummings, Richard D. Development of smart anti-glycan reagents using immunized lampreys |
title | Development of smart anti-glycan reagents using immunized lampreys |
title_full | Development of smart anti-glycan reagents using immunized lampreys |
title_fullStr | Development of smart anti-glycan reagents using immunized lampreys |
title_full_unstemmed | Development of smart anti-glycan reagents using immunized lampreys |
title_short | Development of smart anti-glycan reagents using immunized lampreys |
title_sort | development of smart anti-glycan reagents using immunized lampreys |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7048801/ https://www.ncbi.nlm.nih.gov/pubmed/32111965 http://dx.doi.org/10.1038/s42003-020-0819-2 |
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